Formation of Fe i –B pairs in silicon at high temperatures

We report on the detection of Fe _i –B pairs in heavily B doped silicon using ⁵⁷Fe emission Mössbauer spectroscopy following implantation of radioactive ⁵⁷Mn⁺ parent ions (T _1/2?=?1.5 min) at elevated temperatures >?850 K. The Fe _i –B pairs are formed upon the dissociation of Fe _i –V pairs during the lifetime of the Mössbauer state (T _1/2?=?100 ns). The resulting free interstitial Fe_i diffuses over sufficiently large distances during the lifetime of the Mössbauer state to encounter a substitutional B impurity atom, forming Fe _i –B pairs, which are stable up to ～1,050 K on that time scale.     

Time-domain simulations of sound propagation through screen-induced turbulence

A flow model in combination with a statistical-dynamical turbulence generator and a linearised Euler time-domain model for sound waves were used to simulate the effect of screen-induced turbulence on the noise level in the acoustical shadow of a screen in wind. Instead of simulating a great number of different frozen turbulence realisations, the concept of transient turbulence was successfully tested and applied. This concept is adequate to the time-domain model and reduces the computational demands. Several two-dimensional simulations allowed to isolate the individual effects of wind and screen on the propagation of 500 Hz sound waves over a 4-m high noise barrier. At a distance of 250 m from the source (240 m behind the screen) the sheltering effect of the screen and the refraction effect of the wind are in the order of 6 and 4 dB, respectively. The screen-induced turbulence leads to fluctuations in the noise level with a standard deviation of 1.2 dB and a maximum amplitude of 3 dB. However, the time averaged effect turned out to be in the order of merely 0.2 dB. The effect of the screen-induced turbulence on the average noise level behind the screen is therefore negligible.     

Determination of Hydrogen Single Ion Activity Coefficients in Aqueous HCl Solutions at 25°C

The single ion activity coefficients of hydrogen and chloride ions in aqueous HCl solutions have been estimated at 25°C at concentrations up to 1 mol-kg^–1, using potentiometric measurements with ion-selective electrodes and appropriate calibration procedures. Two methods are described for an internal calibration of the electrodes in the extended Debye–Hückel concentration range. The results are compared to the conventional pH calibration with external buffer solutions. Since the latter calibration method does not account for the liquid junction potential E _J which arises at the reference electrode, the resulting activity coefficients are quite different in HCl solutions of higher concentration. These differences between internal and external calibration decrease significantly, when a correction for E _J is introduced into the conventional pH calibration. Hence, in solutions of higher ionic strength the accuracy of the conventional pH electrode calibration using buffer solutions is very limited, when exact H⁺ activities are required. The consistency of the results indicates that the liquid junction potentials in the examined systems calculated by the Henderson/Bates approximation are of reasonable precision.     

Testing Extreme Value Conditions

A test statistic is developed that checks the validity of the extreme value conditions without specifiying the shape parameter of the limiting extreme value distribution.